Li Tingting, Fu Weihua, Li Xueqi, Huo Yuanqing, Ji Huifang, Liang Taigang, Zhang Ruiping
Medicinal Basic Research Innovation Center of Chronic Kidney Disease, Ministry of Education, Shanxi Medical University, Taiyuan 030001, China.
School of Pharmacy, Shanxi Medical University, Taiyuan 030001, China.
ACS Appl Mater Interfaces. 2025 Jan 8;17(1):386-397. doi: 10.1021/acsami.4c15494. Epub 2024 Dec 18.
Liver fibrosis is a chronic disease that lacks effective drug treatment. Chronic damage and inflammation lead to the formation of collagen and fibrous scars. However, the excessive accumulation of collagen I significantly hinders the delivery of drugs into liver tissue. Therefore, this study developed a quercetin-loaded melanin nanoparticle codecorated collagenase (MNP-QUE-COL) for the treatment of liver fibrosis. These results showed that MNP-QUE-COL degraded excessive collagen I, thereby efficiently delivering melanin and quercetin into the liver tissue. MNP-QUE-COL exhibited optimal PA/MRI dual-mode imaging ability. In addition, the synergistic anti-inflammatory and reactive oxygen species scavenging function of quercetin and melanin was achieved by regulation of M1-M2 macrophage polarization and inhibition of pro-inflammatory cytokine release, reshaping the imbalanced extracellular interstitial inflammatory environment. The results of this research suggest that MNP-QUE-COL is a safe and efficient therapeutic nanoplatform for liver fibrosis, showing promise as a potential therapeutic strategy for liver fibrosis and associated diseases.
肝纤维化是一种缺乏有效药物治疗的慢性疾病。慢性损伤和炎症会导致胶原蛋白和纤维瘢痕的形成。然而,I型胶原蛋白的过度积累显著阻碍了药物向肝组织的递送。因此,本研究开发了一种负载槲皮素的黑色素纳米颗粒共修饰胶原酶(MNP-QUE-COL)用于治疗肝纤维化。这些结果表明,MNP-QUE-COL降解了过量的I型胶原蛋白,从而有效地将黑色素和槲皮素递送至肝组织。MNP-QUE-COL展现出最佳的光声/磁共振成像双模成像能力。此外,槲皮素和黑色素的协同抗炎和清除活性氧功能是通过调节M1-M2巨噬细胞极化以及抑制促炎细胞因子释放来实现的,从而重塑失衡的细胞外间质炎症环境。本研究结果表明,MNP-QUE-COL是一种用于肝纤维化的安全有效的治疗性纳米平台,有望成为肝纤维化及相关疾病的潜在治疗策略。